AmTryke Model 1424 Community Cruiser Hand Cycle — Class II medical device recall Z-1520-2015
Terminated recall by Amtryke LLC, reported 2015-05-06, distributed nationwide. Product is being recalled due to complaints of cracked frames.
| Recall number | Z-1520-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Amtryke LLC, Greensboro, NC, United States |
| Recall initiated | 2015-03-27 |
| Classified | 2015-04-24 |
| Reported by FDA | 2015-05-06 |
| Terminated | 2017-07-10 |
| Distributed | Nationwide (US) |
| Quantity | 53 units |
| Reason classes | packaging |
| Lot numbers | 2-1301, GM-0314 |
| Model numbers | 1424 |
Product
AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle.
Reason for recall
Product is being recalled due to complaints of cracked frames.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1520-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.